Variant report

Variant	rs11952095
Chromosome Location	chr5:124373851-124373852
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1030952	1.00[EUR][1000 genomes]
rs11952059	1.00[EUR][1000 genomes]
rs11952120	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11956205	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1898911	1.00[EUR][1000 genomes]
rs4836148	1.00[EUR][1000 genomes]
rs73306716	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882822	chr5:124250018-124449375	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830474	chr5:124263628-124431299	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124363400-124377600	Weak transcription	Fetal Kidney	kidney
2	chr5:124365400-124379400	Weak transcription	Pancreas	Pancrea
3	chr5:124370600-124377400	Weak transcription	Stomach Mucosa	stomach
4	chr5:124371200-124376600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:124371400-124376400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr5:124371400-124377200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:124371600-124379600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr5:124372600-124374800	Enhancers	Primary B cells from cord blood	blood
9	chr5:124372600-124375000	Enhancers	Primary B cells from peripheral blood	blood
10	chr5:124373200-124374200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:124373200-124374200	Weak transcription	GM12878-XiMat	blood
12	chr5:124373400-124376800	Weak transcription	Dnd41	blood
13	chr5:124373800-124375200	Weak transcription	Adipose Nuclei	Adipose

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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